美国FDA药品数据库-药物在线

商品名	申请号	产品号	申请类型	活性成分	剂型/给药途径	规格/剂量	RLD	RS	申请号原始批准/暂定批准日期	产品号批准日期	申请人	市场状态
DESLORATADINE	078362	001	ANDA	DESLORATADINE	TABLET; ORAL	5MG	No	No	2009/08/24 (TA)	--	GLENMARK GENERICS	None (Tentative Approval)
DESLORATADINE	078357	001	ANDA	DESLORATADINE	TABLET;ORAL	5MG	No	No	2010/02/19	2010/02/19	ORBION PHARMS	Prescription
DESLORATADINE	078367	001	ANDA	DESLORATADINE	TABLET, ORALLY DISINTEGRATING;ORAL	2.5MG	No	No	2010/07/12	2010/07/12	REDDYS	Prescription
DESLORATADINE	078367	002	ANDA	DESLORATADINE	TABLET, ORALLY DISINTEGRATING;ORAL	5MG	No	Yes	2010/07/12	2010/07/12	REDDYS	Prescription
DESLORATADINE	078352	001	ANDA	DESLORATADINE	TABLET;ORAL	5MG	No	No	2010/10/25	2010/10/25	LUPIN PHARMS	Prescription
DESLORATADINE	078359	001	ANDA	DESLORATADINE	TABLET;ORAL	5MG	No	No	2010/11/16	2010/11/16	SUN PHARM INDS	Discontinued
DESLORATADINE	078364	001	ANDA	DESLORATADINE	TABLET;ORAL	5MG	No	No	2010/12/03	2010/12/03	CHARTWELL RX	Discontinued
DESLORATADINE	078365	001	ANDA	DESLORATADINE	TABLET;ORAL	5MG	No	No	2011/03/08	2011/03/08	DR REDDYS LABS LTD	Prescription
DESLORATADINE AND PSEUDOEPHEDRINE SULFATE 24 HOUR	078366	001	ANDA	DESLORATADINE; PSEUDOEPHEDRINE SULFATE	TABLET, EXTENDED RELEASE;ORAL	5MG;240MG	No	Yes	2011/04/26	2011/04/26	DR REDDYS LABS LTD	Prescription
DESLORATADINE	078353	001	ANDA	DESLORATADINE	TABLET; ORAL	5MG	No	No	2011/05/23 (TA)	--	ZYDUS PHARMS USA	None (Tentative Approval)
DESLORATADINE	078361	001	ANDA	DESLORATADINE	TABLET;ORAL	5MG	No	No	2011/12/22	2011/12/22	PERRIGO	Discontinued
DESLORATADINE	078351	001	ANDA	DESLORATADINE	TABLET;ORAL	5MG	No	No	2012/02/10	2012/02/10	DASH PHARMS	Discontinued
DESLORATADINE	078355	001	ANDA	DESLORATADINE	TABLET;ORAL	5MG	No	No	2012/04/19	2012/04/19	BELCHER PHARMS	Prescription
DESLORATADINE	202592	001	ANDA	DESLORATADINE	SOLUTION;ORAL	0.5MG/ML	No	No	2015/06/30	2015/06/30	TARO	Discontinued
DESLORATADINE	202936	001	ANDA	DESLORATADINE	SOLUTION;ORAL	0.5MG/ML	No	No	2016/05/26	2016/05/26	TARO	Discontinued